Curable perfluoropolyether compositions and rubber or gel articles comprising the cured products of the compositions

ABSTRACT

Curable perfluoropolyether rubber compositions are provided comprising (A) a linear perfluoropolyether compound containing at least two alkenyl groups and having a perfluoropolyether structure containing recurring units —C a F 2a O— in its backbone, (B) an organosilicon compound containing at least two SiH groups, (C) an inorganic powder capable of chemical and/or physical adsorption of acidic gases and/or sulfur-containing gases, and (D) a hydrosilylation catalyst. The compositions cure into rubber or gel products having minimal permeability to acidic gases and sulfur-containing gases.

CROSS-REFERENCE TO RELATED APPLICATION

This non-provisional application claims priority under 35 U.S.C. §119(a)on Patent Application No. 2005-035823 filed in Japan on Feb. 14, 2005,the entire contents of which are hereby incorporated by reference.

FIELD OF THE INVENTION

This invention relates to perfluoropolyether rubber or gel compositionswhich cure into products having heat resistance, oil resistance,chemical resistance, solvent resistance, low-temperature properties,moisture resistance, and low gas permeability and especially, minimalacidic gas permeability. The invention also relates to rubber or gelarticles comprising the cured products of the compositions.

BACKGROUND ART

Japanese Patent No. 2,990,646 (JP-A 8-199070) and JP-A 2000-248166disclose a curable composition comprising a linear perfluoropolyethercompound containing at least two alkenyl groups per molecule and havinga perfluoropolyether structure in its backbone, an organosiliconcompound having at least two H—SiOSiO structures per molecule, and ahydrosilylation catalyst, which cures into a product having a goodprofile of heat resistance, chemical resistance, solvent resistance,water repellency, oil repellency and weatherability.

These perfluoropolyether rubber compositions perform well in mostapplications. However, their performance is short in those applicationsrequiring chemical resistance such as sealants in semiconductormanufacturing units, sealants and potting materials for use with engineoil, and sealants and potting materials for use in engine exhaust parts.In such applications, rubber or gel products are urgently desired toprevent or retard electric or electronic parts from corrosion. In somecases, it is necessary to prevent or retard corrosion with acidic gasesand sulfur-containing gases. It is thus strongly desired to haveperfluoropolyether rubber or gel compositions which cure into productshaving oil resistance, chemical resistance, and low gas permeability andespecially, minimal permeability to acidic gases and sulfur-containinggases.

SUMMARY OF THE INVENTION

An object of the invention is to provide curable perfluoropolyetherrubber or gel compositions which when cured, exhibit good heatresistance, solvent resistance, chemical resistance, weatherability,mold release, water repellency and oil repellency and especially minimalpermeability to acidic gases and sulfur-containing gases. Another objectis to provide rubber or gel articles comprising the same.

The inventors have discovered that when an inorganic powder capable ofchemical and/or physical adsorption of acidic gases and/orsulfur-containing gases is incorporated in a perfluoropolyether rubberor gel composition, the resulting composition cures into anon-conductive rubber or gel having a volume resistivity of at least1×10⁹ Ω-cm and exhibiting minimal permeability to acidic gases andsulfur-containing gases. When electric or electronic parts are coveredwith the composition, the inorganic powder serves to react with oradsorb acidic gases or sulfur-containing gases for thereby preventing orretarding the electric or electronic parts from corrosion with suchgases.

Accordingly, in one aspect, the present invention provides a curableperfluoropolyether rubber composition comprising:

(A) 100 parts by weight of a linear perfluoropolyether compoundcontaining at least two alkenyl groups per molecule and having aperfluoropolyether structure containing recurring units —C_(a)F_(2a)O—wherein a is an integer of 1 to 6 in its backbone,

(B) a curing amount of an organosilicon compound containing at least twosilicon-bonded hydrogen atoms per molecule,

(C) 0.1 to 50 parts by weight of an inorganic powder capable of chemicaland/or physical adsorption of acidic gases and/or sulfur-containinggases, and

(D) a catalytic amount of a hydrosilylation catalyst, said compositionbeing cured into a rubber.

In another aspect, the present invention provides a perfluoropolyethercomposition comprising:

(A) 25 to 65 parts by weight of a linear perfluoropolyether compoundcontaining at least two alkenyl groups per molecule and having aperfluoropolyether structure containing recurring units —C_(a)F_(2a)O—wherein a is an integer of 1 to 6 in its backbone,

(E) 75 to 35 parts by weight of a polyfluoromonoalkenyl compoundcontaining one alkenyl group per molecule and having aperfluoropolyether structure in its backbone,

the total amount of components (A) and (E) being 100 parts by weight,

(B) a curing amount of an organosilicon compound containing at least twosilicon-bonded hydrogen atoms per molecule,

(C) 0.1 to 50 parts by weight of an inorganic powder capable of chemicaland/or physical adsorption of acidic gases and/or sulfur-containinggases, and

(D) a catalytic amount of a hydrosilylation catalyst,

said composition being cured into a gel.

In this case, component (E) is preferably a polyfluoromonoalkenylcompound having the general formula (2):Rf¹—(X′)_(p)—CH═CH₂  (2)wherein X′ and p are as defined below, Rf¹ is a group of the generalformula:F—[CF(CF₃)CF₂O]_(w)—CF(CF₃)—wherein w is an integer of 1 to 500.

Preferably, component (A) is a linear perfluoropolyether compound havingthe general formula (1):

wherein X is —CH₂—, —CH₂O—, —CH₂OCH₂— or —Y—NR¹—CO— wherein Y is —CH₂—or a dimethylphenylsilylene group of the structural formula (Z):

(inclusive of o-, m- and p-positions), and R¹ is hydrogen, methyl,phenyl or allyl,

X′ is —CH₂—, —OCH₂—, —CH₂OCH₂— or —CO—NR²—Y— wherein Y is —CH₂— or adimethylphenylsilylene group of the structural formula (Z′):

(inclusive of o-, m- and p-positions), and R² is hydrogen, methyl,phenyl or allyl,

p is independently 0 or 1, r is an integer of 2 to 6, m and n each arean integer of 0 to 600, the sum of m+n is 50 to 600.

Component (C) is preferably a metal powder such as copper, a powderedactive carbon having porosity, or a powdered compound havinghydrotalcite structure.

The composition preferably further comprises (F) at least one linearpolyfluoro compound selected from the class consisting of compoundshaving the general formula (3):A-O—(CF₂CF₂CF₂O)_(d)-A  (3)wherein A is a group of C_(e)F_(2e+1)— wherein e is 1 to 3, and d is aninteger of 1 to 500, and compounds having the general formula (4):A-O—(CF₂O)_(f)(CF₂CF₂O)_(h)-A  (4)wherein A is as defined above, and f and h each are an integer of 1 to300.

The cured products of the compositions preferably have a volumeresistivity of at least 1×10⁹ Ω-cm.

The present invention also provides an above composition in the curedstate, especially for use in automobiles, chemical plants, ink jetprinters, semiconductor manufacturing lines, analytical and scientificinstruments, medical equipment, aircraft or fuel cells.

The present invention further provides a pressure sensor for use inautomobiles comprising a sensor section for detecting a pressure andgenerating an electric signal in response to the detected pressurevalue, and a protective member with chemical resistance covering thesensor section for protection, said protective member comprising theabove perfluoropolyether composition.

BENEFITS OF THE INVENTION

The perfluoropolyether compositions of the invention cure into rubber orgel products that exhibit good heat resistance, oil resistance, chemicalresistance, solvent resistance, low-temperature properties, moistureresistance and low gas permeability, and especially minimal permeabilityto acidic gases and sulfur-containing gases.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic cross-sectional view of a corrosion test setup.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

Component A

Component (A) of the curable perfluoropolyether compositions accordingto the invention is a linear perfluoropolyether compound containing atleast two alkenyl groups per molecule and having a perfluoropolyetherstructure, preferably divalent perfluoroalkylether structure, in itsbackbone.

The perfluoroalkyl ether structures include structures comprising aplurality of recurring units —C_(a)F_(2a)O— wherein a is at eachoccurrence an integer of 1 to 6, for example, structures represented bythe general formula (5):(C_(a)F_(2a)O)_(q)  (5)wherein q is an integer of 50 to 600, preferably 50 to 400, morepreferably 50 to 200.

Examples of the recurring units —C_(a)F_(2a)O— are:—CF₂O—, —CF₂CF₂O—, —CF₂CF₂CF₂O—,—CF(CF₃)CF₂O—, —CF₂CF₂CF₂CF₂O—,—CF₂CF₂CF₂CF₂CF₂CF₂O—, and —C(CF₃)₂O—.Of these, —CF₂O—, —CF₂CF₂O—, —CF₂CF₂CF₂O—, and —CF(CF₃)CF₂O— arepreferred. It is understood that the perfluoroalkyl ether structure mayconsist of recurring units —C_(a)F_(2a)O— of one type or recurring unitsof two or more types.

The alkenyl groups in the linear perfluoropolyether compound (A) arepreferably those groups having 2 to 8 carbon atoms, especially 2 to 6carbon atoms, and terminated with a CH₂═CH— structure, for example,vinyl, allyl, propenyl, isopropenyl, butenyl, and hexenyl. Of these,vinyl and allyl are preferred. The alkenyl groups may be attached to thebackbone of perfluoropolyether compound at both ends either directly orthrough divalent linkages such as —CH₂—, —CH₂O— or —Y—NR—CO—. Herein Yis —CH₂— or a dimethylphenylsilylene group of the formula (Z):

(inclusive of o-, m- and p-positions), and R is hydrogen, methyl, phenylor allyl. There should be included at least two alkenyl groups permolecule.

Suitable perfluoropolyether compounds (A) include polyfluorodialkenylcompounds of the general formulae (6) and (7).CH₂═CH—(X)_(p)—Rf²—(X′)_(p)—CH═CH₂  (6)CH₂═CH—(X)_(p)-Q-Rf²-Q-(X′)_(p)—CH═CH₂  (7)In formulae (6) and (7), X is independently —CH₂—, —CH₂O—, —CH₂OCH₂— or—Y—NR¹—CO— wherein Y is —CH₂— or a dimethylphenylsilylene group of thestructural formula (Z) and R¹ is hydrogen, methyl, phenyl or allyl. X′is —CH₂—, —OCH₂—, —CH₂OCH₂— or —CO—NR²—Y′— wherein Y′ is —CH₂— or adimethylphenylsilylene group of the structural formula (Z′) and R² ishydrogen, methyl, phenyl or allyl.

(inclusive of o-, m- and p-positions)

(inclusive of o-, m- and p-positions)Rf² is a divalent perfluoropolyether structure, and preferably one ofthe formula (5): (C_(a)F_(2a)O)_(q). Q is a divalent hydrocarbon grouphaving 1 to 15 carbon atoms which may contain an ether bond, forexample, an alkylene group or an alkylene group containing an etherbond. The letter p is independently 0 or 1.

The linear perfluoropolyether compound serving as component (A) is mostpreferably a compound of the general formula (1).

Herein, X, X′ and p are as defined above, r is an integer of 2 to 6,each of m and n is an integer of 0 to 600, and the sum of m+n is 50 to600.

The linear perfluoropolyether compound of formula (1) should desirablyhave a weight-average molecular weight (Mw) of 10,000 to 100,000, andmost preferably 10,000 to 50,000 by gel permeation chromatography (GPC)based on polystyrene standard. Compounds with Mw of less than 10,000undergo substantial swell in gasoline and other solvents, asdemonstrated by a swell factor of at least 6% in gasoline, failing tomeet the requirements of parts that must be gasoline resistant.Compounds with Mw of more than 100,000 are too viscous to work,detracting from practical utility.

Illustrative examples of the linear perfluoropolyether compound offormula (1) are given below.

Note that each of m and n is an integer of 0 to 600, preferably 0 to200, and the sum of m+n is 50 to 600, preferably 50 to 200.

In the practice of the invention, to modify the linearperfluoropolyether compound of formula (1) to the desired weight-averagemolecular weight in accordance with the intended use, the linearperfluoropolyether compound may be previously subjected tohydrosilylation with an organosilicon compound bearing two SiH groups ina molecule by an ordinary method and under ordinary conditions. Theresulting chain-extended product can be used as component (A).

Component B

Component (B) is an organosilicon compound having at least two siliconatom-bonded hydrogen atoms (i.e., SiH groups) in a molecule. Theorganosilicon compound (B) serves as a crosslinking agent and chainextender for component (A). When compatibility with and dispersion incomponent (A) and components (E) and (F) to be described later anduniformity after curing are taken into account, the organosiliconcompound should preferably have at least one monovalent perfluoroalkyl,monovalent perfluorooxyalkyl, divalent perfluoroalkylene or divalentperfluorooxyalkylene group in a molecule.

Suitable organosilicon compounds include, but are not limited to,well-known organosilicon compounds as described in the above-referredJP-A 8-199070 and JP-A 2000-248166.

Preferred are cyclic organosilicon compounds of the general formula (8).

Herein Rf³ is a monovalent perfluoroalkyl or perfluoropolyether group,R³ is a monovalent hydrocarbon group of 1 to 20 carbon atoms, R⁴ is adivalent hydrocarbon group of 2 to 20 carbon atoms which may contain anether bond, amido bond, carbonyl bond or ester bond, k is an integer ofat least 2, 1 is an integer of 1 to 6, and the sum of k+1 is 3 to 10.

Examples of monovalent perfluoroalkyl or perfluoropolyether groupsrepresented by Rf³ include monovalent perfluoroalkyl groups:C_(b)F_(2b+1)— wherein b is an integer from 1 to 20, and preferably from2 to 10 and monovalent perfluorooxyalkyl groups:

wherein n is an integer from 2 to 200, preferably 2 to 100.

R³ is a monovalent hydrocarbon group of 1 to 20 carbon atoms, preferably1 to 12 carbon atoms, for example, alkyl groups such as methyl, ethyl,propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, hexyl, octyl anddecyl; cycloalkyl groups such as cyclopentyl, cyclohexyl andcycloheptyl; alkenyl groups such as vinyl, allyl, propenyl, isopropenyl,butenyl and hexenyl; aryl groups such as phenyl, tolyl, xylyl andnaphthyl; and aralkyl groups such as benzyl, phenylethyl, phenylpropyl.Of these, those free of aliphatic unsaturation are preferred.

R⁴ is a divalent hydrocarbon group of 2 to 20 carbon atoms which maycontain an ether bond, amido bond, carbonyl bond or ester bond. Suchdivalent linking groups include alkylene groups, arylene groups, andcombinations thereof, in which may intervene an ether-bonding oxygenatom (—O—), an amide bond (—NRCO— wherein R is hydrogen atom, an alkylgroup of 1 to 4 carbon atoms or phenyl group), a carbonyl bond (—CO—),an ester bond (—COO—) or the like, with those of 2 to 12 carbon atomsbeing preferred. Examples of suitable divalent linking groups are:

-   —CH₂CH₂—,-   —CH₂CH₂CH₂—,-   —CH₂CH₂CH₂OCH₂—,-   —CH₂CH₂CH₂—NH—CO—,-   —CH₂CH₂CH₂—N(Ph)—CO—,-   —CH₂CH₂CH₂—N(CH₃)—CO—, and-   —CH₂CH₂CH₂—O—CO—.    Note that Ph is phenyl.

Component (B) is generally included in an amount effective for curingcomponents (A) and (E), specifically an amount of supplying preferably0.2 to 2 moles, and more preferably 0.5 to 1.5 moles, of hydrosilyl(SiH) groups per mole of total alkenyl groups on components (A) and (E).Too little hydrosilyl (SiH) groups may lead to an inadequate degree ofcrosslinking or under-cure, whereas too much may cause foaming duringcuring.

Component C

Component (C) is an inorganic powder capable of chemical and/or physicaladsorption of acidic gases and/or sulfur-containing gases. Suitablepowders include powdered metals and powdered compounds havinghydrotalcite structure, capable of chemical adsorption of acidic gasesand/or sulfur-containing gases, and powdered active carbon havingporosity capable of physical adsorption of acidic gases and/orsulfur-containing gases.

As used herein, “acidic gases” and “sulfur-containing gases” aregenerally known as corrosive gases and include gases of NOx, SOx, aceticacid, formic acid, nitric acid, sulfuric acid, sulfur, and sulfurousacid.

The powdered metal as component (C) enables to prevent or retard acidicgases or sulfur-containing gases from reaching electric or electronicparts by chemically converting acidic gases or sulfur-containing gasesinto oxides or sulfides. Examples of metals having such an effectinclude silver, copper, iron, nickel, aluminum, tin, and zinc. Of these,powdered copper is preferred for stability and cost. The shape andnature of powdered metal are not particularly limited as long as thedesired effect is exerted. In consideration of the impurity content andfluidity of the composition loaded with the powdered metal, atomizedmetal is preferred. Suitable powdered metals are commercially available,for example, under the trade name of copper powder (flake) 3L3 by FukudaMetal Foil Industry Co., Ltd., copper powder (atomized powder) FCC-SP-99by Fukuda Metal Foil Industry Co., Ltd., and iron powder (atomizedpowder) Atomel 300M by Kobe Steel, Ltd.

The powdered compounds having hydrotalcite structure are compounds ofmagnesium and aluminum and have an exchangeability with anions of acidicgases or sulfur-containing gases, enabling to prevent or retard acidicgases or sulfur-containing gases from reaching electric or electronicparts.

With respect to the powdered compounds having hydrotalcite structure,the known hydrotalcites can be used. Numerous proposals for improvingwater-vapor resistance reliability and heat resistance property asion-trapping agents of semiconductor trapping agents are shown inJapanese Patent Nos. 2501820, 2519277, 2712898 and 3167853, JP-B06-051826, JP-A 09-118810, JP-A 10-158360, JP-A 11-240937, JP-A11-310766, JP-A 2000-159520, JP-A 2000-230110, and JP-A 2002-080566. Anyhydrotalcite described in the above patent documents can be used.

Especially, the compound represented by the general formula (9) can beused as the powdered compound having hydrotalcite structure:Mg_(x)Al_(y)(OH)_(2x+3y+2z)(CO₃)_(z).αH₂Owherein x, y and z have the relationship of 0<y/x≦1 and 0≦z/y<1.5, and αis an integer.

Examples of the powdered compounds having hydrotalcite structure include1.25Mg(OH)₂.Al(OH)₃.zCO₃.αH₂O,Mg₆Al₂(OH)₁₆CO₃.4H₂O, andMg_(4.5)Al₂(OH)₁₃CO₃.3.5H₂O.

Hydrotalcite has an anion exchangeability. In contact with HCl gas, forexample, chemical adsorption occurs according to the reaction schemebelow.Mg₆Al₂(OH)₁₆CO₃.4H₂O+2HCl→Mg₆Al₂(OH)₁₃Cl₂.nH₂O+H₂O+CO₂

The powdered compounds having hydrotalcite structure are commerciallyavailable, for example, under the trade name of Kyoward 500, Kyoward1000 and DHT-4A-2 by Kyowa Chemical Industry Co., Ltd.

A further embodiment of the inorganic powder capable of physicaladsorption of acidic gases and/or sulfur-containing gases is powderedactive carbon having porosity. It is capable of selective adsorption ofacidic gases or sulfur-containing gases within the porous structure,enabling to prevent or retard acidic gases or sulfur-containing gasesfrom reaching electric or electronic parts. Examples of the powderedactive carbon include steam-activated carbon produced from wooden rawmaterials by steam activation and zinc chloride-activated carbonproduced by chemical activation and purification. The powdered activecarbon with porosity is commercially available, for example, under thetrade name of activated carbon Shirasagi grades A, C, M and P by NipponEnviro-Chemicals, Ltd.

The amount of the inorganic powder (C) added should be enough to achievethe desired effect of preventing or retarding acidic gases orsulfur-containing gases from reaching electric or electronic parts andis typically 0.1 to 50 parts by weight per 100 parts by weight ofcomponent (A) or components (A) and (E) combined. For the fluidity ofthe composition and the volume resistivity of the cured composition, thepreferred amount of the inorganic powder is 0.3 to 30 parts by weight,even more preferably 0.5 to 20 parts by weight.

If the cured perfluoropolyether composition is electroconductive or hasa volume resistivity of less than 1×10 ⁹ Ω-cm, the composition isunacceptable in coating electric or electronic parts therewith. It isnecessary to maintain a certain volume resistivity. Thus the type andamount of the inorganic powder should be selected so that the curedperfluoropolyether composition has a volume resistivity of equal to ormore than 1×10⁹ Ω-cm, especially equal to or more than 1×10¹⁰ Ω-cm.

Component D

Component (D) is a hydrosilylation catalyst which promotes additionreaction between alkenyl groups in components (A) and (E) and hydrosilylgroups in component (B). The hydrosilylation catalysts are typicallynoble metal compounds which are expensive. Platinum and platinumcompounds are thus used because they are readily available.

Exemplary platinum compounds include chloroplatinic acid, complexes ofchloroplatinic acid with olefins such as ethylene, complexes ofchloroplatinic acid with alcohols and vinylsiloxanes, and metallicplatinum supported on silica, alumina or carbon, though are not limitedthereto. Known platinum group metal compounds other than the platinumcompounds include rhodium, ruthenium, iridium, and palladium compounds,for example, RhCl(PPh₃)₃, RhCl(CO)(PPh₃)₂, Ru₃(CO)₁₂, IrCl(CO)(PPh₃) 2,and Pd(PPh₃)₄ wherein Ph denotes phenyl.

The amount of the hydrosilylation catalyst used may be a catalyticamount, and preferably an amount to give 0.1 to 100 ppm of platinumgroup metal based on the total weight of components (A), (B) and (E).

Component E

Component (E) is a polyfluoromonoalkenyl compound containing one alkenylgroup per molecule and having a perfluoropolyether structure in itsbackbone. It is preferably a polyfluoromonoalkenyl compound having thegeneral formula (2):Rf¹-(X′)_(p)—CH═CH₂  (2)wherein X′ and p are as defined above, Rf¹ is a group of the generalformula:F-[CF(CF₃)CF₂O]_(w)—CF(CF₃)—wherein w is an integer of 1 to 500, preferably 2 to 200.

Illustrative examples of the polyfluoromonoalkenyl compound havingformula (2) are given below.

Herein m is an integer of 1 to 200, preferably 2 to 100.

In the curable perfluoropolyether gel composition, an amount of thepolyfluoromonoalkenyl compound (E) having formula (2) compounded isselected so that the amount of component (A) or the linearperfluoropolyether compound containing at least two alkenyl groups permolecule is 25 to 65 parts by weight and the amount of component (E) orthe polyfluoromonoalkenyl compound containing one alkenyl group permolecule is 75 to 35 parts by weight, and the total amount of components(A) and (E) is 100 parts by weight.

Component F

Regardless of whether it is a rubber or gel composition, theperfluoropolyether composition of the invention may further comprise (F)a nonfunctional fluoropolymer having a perfluoropolyether structurecomprising recurring units —C_(a)F_(2a)O— wherein a is as defined above,but free of alkenyl groups. This nonfunctional fluoropolymer is mostpreferably linear.

The linear perfluoropolyether compound, when compounded as component(F), serves to improve chemical resistance, solvent resistance andlow-temperature properties without detracting from physical properties.Particularly when it is compounded in perfluoropolyether rubber and gelcompositions, it is effective for imparting improved low-temperatureproperties, typically lowering the glass transition temperature.

Component (F) is preferably at least one linear perfluoropolyethercompound selected from the class consisting of compounds having thegeneral formula (3):A-O-(CF₂CF₂CF₂O)_(d)-A  (3)wherein A is a group of C_(e)F_(2e+1)— wherein e is 1 to 3, and d is aninteger of 1 to 500, preferably 2 to 200, and compounds having thegeneral formula (4):A-O—(CF₂O)_(f)(CF₂CF₂O)_(h)-A  (4)wherein A is as defined above, and f and h each are an integer of 1 to300, preferably 1 to 100.

Illustrative examples of component (F) are:CF₃O—(CF₂CF₂CF₂O), —CF₂CF₃ andCF₃—[(OCF₂CF₂)_(n). (OCF₂)_(m).]—O—CF₃wherein m′ is an integer of 1 to 200, n′ is an integer of 1 to 200, andm′+n′ is 1 to 200.

An appropriate amount of component (F) compounded varies whether theperfluoropolyether composition is a rubber or gel composition. In theperfluoropolyether gel composition, the preferred amount of component(F) is 20 to 100 parts by weight per 100 parts by weight of components(A) and (E) combined, i.e., polyfluorodialkenyl compound pluspolyfluoromonoalkenyl compound. In the perfluoropolyether rubbercomposition, the preferred amount of component (F) is 10 to 50 parts byweight per 100 parts by weight of component (A). Component (F) may beone or more of suitable compounds.

Other Components

In addition to components (A) to (F) described above, the compositionsof the invention may further comprise various additives. Suitablehydrosilylation catalyst regulators include acetylenic alcohols such as1-ethynyl-1-hydroxycyclohexane, 3-methyl-1-butyn-3-ol,3,5-dimethyl-1-hexyn-3-ol, 3-methyl-1-penten-3-ol and phenylbutynol;3-methyl-3-penten-1-yne and 3,5-dimethyl-3-hexen-1-yne;polymethylvinylsiloxane cyclic compounds; and organophosphoruscompounds. The addition of such regulators keeps appropriate curereactivity and shelf stability.

Suitable inorganic fillers include fumed silica, fused silica,crystalline silica, iron oxide, zinc oxide, titanium oxide, calciumcarbonate, magnesium carbonate, zinc carbonate, and carbon black. Theaddition of such inorganic fillers adjusts the hardness or mechanicalstrength of cured products of the compositions. Hollow inorganic fillersor spherical rubbery fillers are also useful.

To impart adhesion, any of well-known tackifiers having epoxy, alkoxy orsimilar groups may be added. These additives may be used in any desiredamounts as long as they do not interfere with properties of thecompositions or properties of the cured products.

Cured Products

The perfluoropolyether rubber or gel compositions of the invention cureinto satisfactory products having good heat resistance, chemicalresistance, solvent resistance, water repellency, oil repellency andweatherability and especially low gas permeability, typically minimalpermeability to acidic gases or sulfur-containing gases and thus findinga variety of applications.

The cured perfluoropolyether rubber can be formed by combining 100 partsby weight of component (A) with an amount of component (B) to provide0.2 to 2.0 moles of hydrosilyl groups per mole of total alkenyl groupsin component (A), 0.1 to 50 parts by weight of component (C), and anamount of component (D) to provide 0.1 to 100 ppm of platinum relativeto the total weight of components (A) and (B). To the mix, 10 to 50parts by weight of component (F) may be added if desired for reducingthe glass transition temperature.

The cured rubber is formed by any of prior art well-known techniques,for example, by casting the composition into a suitable mold and causingthe composition to cure therein, by coating the composition onto asuitable substrate and curing it thereto, or by lamination. The curingis readily achieved by heating at a temperature of about 60 to about150° C. for about 30 to about 180 minutes.

The rubber thus cured is typically a rubber material having a hardnessof 10 to 80 according to JIS K6249 and a glass transition temperature ofup to −50° C.

The cured perfluoropolyether gel can be formed by combining 25 to 65parts by weight of component (A) with 75 to 35 parts by weight ofcomponent (E) 100 parts by weight of the total amounts of components (A)and (E), an amount of component (B) to provide 0.2 to 2.0 moles ofhydrosilyl groups per mole of total alkenyl groups in components (A) and(E), 0.1 to 50 parts by weight of component (C), and an amount ofcomponent (D) to provide 0.1 to 100 ppm of platinum relative to thetotal weight of components (A), (B) and (E). To the mix, 20 to 100 partsby weight of component (F) may be added if desired for reducing theglass transition temperature.

The cured gel is formed by any of prior art well-known techniques, forexample, by casting the composition into a suitable mold and causing thecomposition to cure therein, by coating the composition onto a suitablesubstrate and curing it thereto, or by lamination. The curing is readilyachieved by heating at a temperature of about 60 to about 150° C. forabout 30 to about 180 minutes.

The gel thus cured is typically a gel material having a penetration of10 to 150 according to the consistency test (using a ¼ cone) of JISK2220 or ASTM D-1403 and a glass transition temperature of up to −50° C.

Rubber or gel articles comprising the cured perfluoropolyether rubber orgel compositions of the invention are suitable for use in a variety ofapplications, for example, automobiles, chemical plants, ink jetprinters, semiconductor manufacturing lines, analytical or scientificinstruments, medical equipment, aircraft, and fuel cells.

Specifically, rubber or gel articles comprising the curedperfluoropolyether rubber or gel compositions of the invention aresuitable for use as rubber parts for automobiles, rubber parts forchemical plants, rubber parts for ink jet printers, rubber parts forsemiconductor manufacturing lines, rubber parts for analytical andscientific instruments, rubber parts for medical equipment, rubber partsfor aircraft, tent coating materials, sealants, molded parts, extrudedparts, coats, copier roll materials, electrical and electronicmoisture-proof coatings, sensor potting materials, fuel cell sealingmaterials, and laminate rubber fabrics.

More specifically, rubber or gel articles comprising the curedcompositions of the invention include, but are not limited to,

rubber parts for automobiles, for example, diaphragms such as fuelregulator diaphragms, pulsation damper diaphragms, oil pressure switchdiaphragms, and EGR diaphragms, valves such as canister valves and powercontrol valves, O-rings such as quick connector O-rings and injectorO-rings, and seals such as oil seals and cylinder head gaskets;

rubber parts for chemical plants, for example, pump diaphragms, valves,O-rings, packings, oil seals, and gaskets;

rubber parts for ink jet printers and semiconductor manufacturing lines,for example, diaphragms, valves, O-rings, packings, and gaskets;

rubber parts for analytical and scientific instruments and medicalequipment, for example, pump diaphragms, O-rings, packings, valves, andjoints;

rubber parts for aircraft, for example, O-rings, face seals, packings,gaskets, diaphragms, and valves in fluid piping for engine oil, jetfuel, hydraulic oil and Skydrol®;

rubber parts for fuel cells, for example, sealants between electrodes,O-rings, face seals, packings, gaskets, diaphragms, and valves inhydrogen, air and coolant water feed pipes;

electric and electronic moisture-proof coating materials and sensorpotting materials for use in, for example, gas pressure sensors,hydraulic pressure sensors, temperature sensors, humidity sensors,rotation sensors, gravity sensors, timing sensors, air flow meters,electronic circuits, semiconductor modules, and various control units.

In a pressure sensor in which a sensor section for detecting a pressureand generating an electric signal in response to the detected pressurevalue is covered with a protective member with chemical resistance forprotection, the protective member may be made using the curableperfluoropolyether rubber or gel composition of the invention. Whileprior art pressure sensors include those sensors which are used in anenvironment exposed to chemicals such as gasoline, typically vacuumsensors for sensing the pressure in an intake manifold in an automobileand those sensors which are used in an environment exposed to acidicgases such as NOx and SOx, typically automotive exhaust gas pressuresensors and automatic transmission sensors, the coverage with thecurable perfluoropolyether rubber or gel composition of the inventionimproves acid resistance and chemical resistance.

When the inventive compositions are potted or coated onto substrates toform cured products thereon, it is advantageous to use conventionalprimers in order to improve the bond or adhesion of the inventivecompositions to substrates. The use of primers prevents penetration ofchemicals and solvents from the substrate interface, and improves theacid resistance, chemical resistance and solvent resistance of entireparts.

As the primer, use may be made of silane primers based on silanecoupling agents, organohydrogenpolysiloxane-based primers, syntheticrubber-based primers, acrylic resin-based primers, urethane resin-basedprimers, and epoxy resin-based primers. The perfluoropolyether rubbercomposition of the invention having a tackifier added thereto is alsouseful as the primer.

EXAMPLE

Examples are given below by way of illustration and not by way oflimitation. Note that all parts (pbw) and % are by weight.

Examples 1-6 & Comparative Examples 1-5

Using the ingredients identified below, several perfluoropolyetherrubber or gel compositions were prepared as formulated in Table 1.

The rubber or gel compositions were cured under conditions of 150° C.and 1 hour, following which the hardness and volume resistivity of thecured products were measured. Corrosion tests were also carried out. Theresults are also shown in Table 1.

Ingredients

(a) Inorganic powder

-   -   (a-1) gold powder (flake), SA05 by Ishifuku Metal Co., Ltd.    -   (a-2) copper powder (flake), 3L3 by Fukuda Metal Foil Industry        Co., Ltd.    -   (a-3) copper powder (atomized powder), FCC-SP-99 by Fukuda Metal        Foil Industry Co., Ltd.    -   (a-4) iron powder (atomized powder), Atomel 300M by Kobe Steel,        Ltd.    -   (a-5) active carbon, Shirasagi A by Nippon Enviro-Chemicals,        Ltd.    -   (a-6) synthetic hydrotalcite, Kyoward 500 by Kyowa Chemical        Industry Co., Ltd.    -   (a-7) synthetic hydrotalcite, Kyoward 1000 by Kyowa Chemical        Industry Co., Ltd.    -   (a-8) fumed silica, Aerosil R-972 by Nippon Aerosil Co., Ltd.

(b) Perfluoropolyether oil

(d) Catalyst, toluene solution of platinum-divinyltetramethyldisiloxanecomplex (platinum content 0.5%)

(e) Curing regulator, 50% toluene solution of ethynyl cyclohexanol

(f) Fluorosilicone gel based on trifluoropropyl-bearing silicone, FE57by Shin-Etsu Chemical Co., Ltd.

(g) Silicone gel based on dimethylsilicone, KE1052 by Shin-Etsu ChemicalCo., Ltd.

Corrosion Test A

As shown in FIG. 1, a glass bottle 1 receives a silver-plated copperplate 2. A dimethylsilicone gel 3 is potted and cured to bury the copperplate 2 therein. A perfluoropolyether composition 4 is cured on the gel3 to a thickness of 3 mm. A polyethylene container 5 having 0.10 g ofsulfur powder received therein is rested on the perfluoropolyethercomposition 4. The bottle 1 is sealed with a metal cap 7. The bottle 1was held in a thermostat chamber at 80° C. for 28 days, after which thesilver plating was visually observed to see how it was corroded. Thesample is rated good (∘) for no corrosion and unacceptable (X) when itis corroded or blackened.

Corrosion Test B

As shown in FIG. 1, a glass bottle 1 receives a silver-plated copperplate 2. A dimethylsilicone gel 3 is potted and cured to bury the copperplate 2 therein. A perfluoropolyether composition 4 is cured on the gel3 to a thickness of 3 mm. A polyethylene container 5 having 0.30 g of36% aqueous hydrochloric acid received therein is rested on theperfluoropolyether composition 4. The bottle 1 is sealed with a metalcap 7. The bottle 1 was held in a thermostat chamber at 80° C. for 28days, after which the silver plating was visually observed to see how itwas corroded. The sample is rated good (∘) for no corrosion andunacceptable (X) when it is corroded or blackened. TABLE 1 ExampleComparative Example Ingredients (pbw) 1 2 3 4 5 6 1 2 3 4 5 a-1 goldpowder (flake) 5 a-2 copper powder (flake) 5 a-3 copper powder(atomized) 5 5 5 a-4 iron powder (atomized) 5 a-5 active carbon 1 a-6Kyoward 500 2 a-7 Kyoward 1000 3 a-8 fumed silica 5 b-1Perfluoropolyether 1 100 100 100 55 55 55 100 100 55 b-2Perfluoropolyether 2 20 20 20 20 b-3 Perfluoropolyether 3 25 25 25 25c-1 Hydrosiloxane 1 2 2 2 2 2 c-2 Hydrosiloxane 2 20 20 20 20 d Ptcompound 0.2 0.2 0.2 0.12 0.12 0.12 0.2 0.2 0.12 e curing regulator 0.30.3 0.3 0.15 0.15 0.15 0.3 0.3 0.15 f FE-57 100 g KE1052 100 HardnessJIS K6249 38 40 38 37 46 (Durometer A) Hardness JIS K2220 78 82 76 78 5762 (Penetration) Corrosion Initial ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ test A after 28days ◯ ◯ ◯ ◯ ◯ ◯ X X X X X Corrosion Initial ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ ◯ testB after 28 days ◯ ◯ ◯ ◯ ◯ ◯ X X X X X Volume resistivity (Ω · cm) 2 × 1× 1 × 5 × 2 × 4 × 1 × 6 × 2 × 3 × 2 × 10¹⁴ 10¹⁴ 10¹⁴ 10¹⁴ 10¹⁰ 10¹⁴ 10¹⁴10¹⁴ 10¹⁴ 10¹² 10¹⁵

Japanese Patent Application No. 2005-035823 is incorporated herein byreference.

Although some preferred embodiments have been described, manymodifications and variations may be made thereto in light of the aboveteachings. It is therefore to be understood that the invention may bepracticed otherwise than as specifically described without departingfrom the scope of the appended claims.

1. A curable perfluoropolyether composition comprising: (A) 100 parts byweight of a linear perfluoropolyether compound containing at least twoalkenyl groups per molecule and having a perfluoropolyether structurecontaining recurring units —C_(a)F_(2a)O— wherein a is an integer of 1to 6 in its backbone, (B) a curing amount of an organosilicon compoundcontaining at least two silicon-bonded hydrogen atoms per molecule, (C)0.1 to 50 parts by weight of an inorganic powder capable of chemicaland/or physical adsorption of acidic gases and/or sulfur-containinggases, and (D) a catalytic amount of a hydrosilylation catalyst, saidcomposition being cured into a rubber.
 2. The composition of claim 1wherein component (C) is a metal powder.
 3. The composition of claim 2wherein component (C) is copper.
 4. The composition of claim 1 whereincomponent (C) is a powdered active carbon having porosity.
 5. Thecomposition of claim 1 wherein component (C) is a powdered compoundhaving hydrotalcite structure.
 6. The composition of claim 1, whereincomponent (A) is a linear perfluoropolyether compound having the generalformula (1):

wherein X is —CH₂—, —CH₂O—, —CH₂OCH₂— or —Y—NR¹—CO— wherein Y is —CH₂—or a dimethylphenylsilylene group of the structural formula (Z):

(inclusive of o-, m- and p-positions), and R¹ is hydrogen, methyl,phenyl or allyl, X′ is —CH₂—, —OCH₂—, —CH₂OCH₂— or —CO—NR²—Y— wherein Yis —CH₂— or a dimethylphenylsilylene group of the structural formula(Z′):

(inclusive of o-, m- and p-positions), and R² is hydrogen, methyl,phenyl or allyl, p is independently 0 or 1, r is an integer of 2 to 6, mand n each are an integer of 0 to 600, the sum of m+n is 50 to
 600. 7.The composition of claim 1, further comprising (F) at least one linearpolyfluoro compound selected from the class consisting of compoundshaving the general formula (3):A-O—(CF₂CF₂CF₂O)_(d)-A  (3) wherein A is a group of C_(e)F_(2e+1)—wherein e is 1 to 3, and d is an integer of 1 to 500, and compoundshaving the general formula (4):A-O—(CF₂O)_(f)(CF₂CF₂O)_(h)-A (4) wherein A is as defined above, and fand h each are an integer of 1 to
 300. 8. The composition of claim 1,which cures into a non-conductive rubber having a volume resistivity ofat least 1×10⁹ Ω-cm.
 9. A rubber article comprising the composition ofclaim 1 in the cured state.
 10. A rubber article comprising thecomposition of claim 1 in the cured state, for use in automobiles,chemical plants, ink jet printers, semiconductor manufacturing lines,analytical and scientific instruments, medical equipment, aircraft orfuel cells.
 11. A pressure sensor for use in automobiles comprising asensor section for detecting a pressure and generating an electricsignal in response to the detected pressure value, and a protectivemember with chemical resistance covering the sensor section forprotection, said protective member comprising the perfluoropolyethercomposition of claim
 1. 12. A curable perfluoropolyether compositioncomprising: (A) 25 to 65 parts by weight of a linear perfluoropolyethercompound containing at least two alkenyl groups per molecule and havinga perfluoropolyether structure containing recurring units —C_(a)F_(2a)O—wherein a is an integer of 1 to 6 in its backbone, (E) 75 to 35 parts byweight of a polyfluoromonoalkenyl compound containing one alkenyl groupper molecule and having a perfluoropolyether structure in its backbone,the total amount of components (A) and (E) being 100 parts by weight,(B) a curing amount of an organosilicon compound containing at least twosilicon-bonded hydrogen atoms per molecule, (C) 0.1 to 50 parts byweight of an inorganic powder capable of chemical and/or physicaladsorption of acidic gases and/or sulfur-containing gases, and (D) acatalytic amount of a hydrosilylation catalyst, said composition beingcured into a gel.
 13. The composition of claim 12 wherein component (C)is a metal powder.
 14. The composition of claim 13 wherein component (C)is copper.
 15. The composition of claim 12 wherein component (C) is apowdered active carbon having porosity.
 16. The composition of claim 12wherein component (C) is a powdered compound having hydrotalcitestructure.
 17. The composition of claim 12, wherein component (A) is alinear perfluoropolyether compound having the general formula (1):

wherein X is —CH₂—, —CH₂O—, —CH₂OCH₂— or —Y—NR¹—CO— wherein Y is —CH₂—or a dimethylphenylsilylene group of the structural formula (Z):

(inclusive of o-, m- and p-positions), and R¹ is hydrogen, methyl,phenyl or allyl, X′ is —CH₂—, —OCH₂—, —CH₂OCH₂— or —CO—NR²—Y— wherein Yis —CH₂— or a dimethylphenylsilylene group of the structural formula(Z′):

(inclusive of o-, m- and p-positions), and R² is hydrogen, methyl,phenyl or allyl, p is independently 0 or 1, r is an integer of 2 to 6, mand n each are an integer of 0 to 600, the sum of m+n is 50 to
 600. 18.The composition of claim 12, wherein component (E) is apolyfluoromonoalkenyl compound having the general formula (2):Rf¹—(X′)_(p)—CH═CH₂  (2) wherein X′ and p are as defined above, Rf¹ is agroup of the general formula:F-[CF(CF₃)CF₂O]_(w)—CF(CF₃)— wherein w is an integer of 1 to
 500. 19.The composition of claim 12, further comprising (F) at least one linearpolyfluoro compound selected from the class consisting of compoundshaving the general formula (3):A-O—(CF₂CF₂CF₂O)d-A  (3) wherein A is a group of C_(e)F_(2e+1)— whereine is 1 to 3, and d is an integer of 1 to 500, and compounds having thegeneral formula (4):A-O—(CF₂O)_(f)(CF₂CF₂O)_(h)—A  (4) wherein A is as defined above, and fand h each are an integer of 1 to
 300. 20. The composition of claim 12,which cures into a non-conductive gel having a volume resistivity of atleast 1×10⁹ Ω-cm.
 21. A gel article comprising the composition of claim12 in the cured state.
 22. A gel article comprising the composition ofclaim 12 in the cured state, for use in automobiles, chemical plants,ink jet printers, semiconductor manufacturing lines, analytical andscientific instruments, medical equipment, aircraft or fuel cells.
 23. Apressure sensor for use in automobiles comprising a sensor section fordetecting a pressure and generating an electric signal in response tothe detected pressure value, and a protective member with chemicalresistance covering the sensor section for protection, said protectivemember comprising the perfluoropolyether composition of claim 12.